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Differential
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anticonvulsants
anticonvulsants, selection of
ataxia
ataxic gait
basal ganglia, calcification of
cardiomyopathy
CAT scan
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebral cortical atrophy
cerebral glucose metabolism
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
children
chronic progressive external ophthalmoplegia
coenzyme Q10 deficiency
dementia
dentatorubral-pallidoluysian atrophy
diabetes mellitus
dystonia
Ekbom's Syndrome
encephalopathy
falling
gene therapy
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genetic neurologic disorders
genetic testing
headache
hearing loss
heart block
intellectual deterioration
intestinal pseudoobstruction
Kearns-Sayre syndrome
Lafora's disease
Leber's hereditary optic neuropathy
Leigh's disease
leukocyte enzyme abnormality
MELAS syndrome
memory, impairment of
MERRF syndrome
mimics
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
MRI
MRI, abnormal
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathy
neuropathy, ataxia, retinitis pigmentosa
ophthalmoplegia
ophthalmoplegia, progressive external
optic neuropathy
pancytopenia
pigmentary retinopathy
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
ptosis
ragged-red fibers
retinopathy
review article
seizure
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
short stature
symmetric brain lesions
treatment of neurologic disorder
Unverricht-Lundborg disease
weight loss
white matter disease
Showing articles 0 to 7 of 7

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988



Showing articles 0 to 7 of 7